Package 76420-074-30

Brand: finasteride

Generic: finasteride
NDC Package

Package Facts

Identity

Package NDC 76420-074-30
Digits Only 7642007430
Product NDC 76420-074
Product ID 76420-074_ead2d1fe-f89c-ee3a-e053-2995a90ac920
Description

30 TABLET, FILM COATED in 1 BOTTLE (76420-074-30)

Marketing

Marketing Status
Marketed Since 2020-01-04
Brand finasteride
Generic finasteride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ead2d1fe-f89c-ee3a-e053-2995a90ac920", "openfda": {"nui": ["N0000175836", "N0000000126"], "unii": ["57GNO57U7G"], "rxcui": ["200172"], "spl_set_id": ["b63af2cd-5c12-4977-bac4-95e1eae11e57"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76420-074-30)", "package_ndc": "76420-074-30", "marketing_start_date": "20200104"}], "brand_name": "Finasteride", "product_id": "76420-074_ead2d1fe-f89c-ee3a-e053-2995a90ac920", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "76420-074", "generic_name": "Finasteride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Finasteride", "active_ingredients": [{"name": "FINASTERIDE", "strength": "1 mg/1"}], "application_number": "ANDA090060", "marketing_category": "ANDA", "marketing_start_date": "20130701", "listing_expiration_date": "20261231"}